Product NDC: | 0536-3606 |
Proprietary Name: | Childrens Pain and Fever Acetaminophen |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0536-3606 |
Labeler Name: | Rugby |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120824 |
Package NDC: | 0536-3606-96 |
Package Description: | 60 mL in 1 BOTTLE (0536-3606-96) |
NDC Code | 0536-3606-96 |
Proprietary Name | Childrens Pain and Fever Acetaminophen |
Package Description | 60 mL in 1 BOTTLE (0536-3606-96) |
Product NDC | 0536-3606 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20120824 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rugby |
Substance Name | ACETAMINOPHEN |
Strength Number | 160 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |